Variant report

Variant	nsv521136
Chromosome Location	chr9:95782667-95798871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:95790645-95791054	GM12878	blood:	n/a	n/a
2	BCL3	chr9:95790609-95791018	GM12878	blood:	n/a	n/a
3	BCLAF1	chr9:95790719-95791131	GM12878	blood:	n/a	n/a
4	BHLHE40	chr9:95798480-95798523	K562	blood:	n/a	n/a
5	BHLHE40	chr9:95792085-95792137	K562	blood:	n/a	n/a
6	BHLHE40	chr9:95794958-95795127	HepG2	liver:	n/a	n/a
7	BHLHE40	chr9:95796270-95796590	K562	blood:	n/a	n/a
8	BHLHE40	chr9:95794853-95795222	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:95783208-95783348	IMR90	lung:	n/a	n/a
10	CEBPB	chr9:95783255-95783446	A549	lung:	n/a	n/a
11	CEBPB	chr9:95783223-95783423	HepG2	liver:	n/a	n/a
12	CTCF	chr9:95798460-95798579	Gliobla	brain:	n/a	n/a
13	CTCF	chr9:95786424-95786460	Spleen_OC	spleen:	n/a	n/a
14	CTCF	chr9:95798251-95798639	K562	blood:	n/a	n/a
15	CTCF	chr9:95798320-95798470	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr9:95798520-95798670	HCM	heart:	n/a	n/a
17	CTCF	chr9:95798380-95798530	MCF-7	breast:	n/a	n/a
18	CTCF	chr9:95798480-95798630	GM12869	blood:	n/a	n/a
19	CTCF	chr9:95798340-95798490	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr9:95783133-95783181	GM13977	blood:	n/a	n/a
21	CTCF	chr9:95798444-95798596	MCF-7	breast:	n/a	n/a
22	CTCF	chr9:95798425-95798610	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr9:95798400-95798550	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr9:95798406-95798580	HepG2	liver:	n/a	n/a
25	CTCF	chr9:95790780-95790930	NB4	blood:	n/a	n/a
26	CTCF	chr9:95783100-95783250	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr9:95798440-95798590	GM12870	blood:	n/a	n/a
28	CTCF	chr9:95798420-95798570	GM12872	blood:	n/a	n/a
29	CTCF	chr9:95798447-95798546	GM10266	blood:	n/a	n/a
30	CTCF	chr9:95798460-95798610	GM12864	blood:	n/a	n/a
31	CTCF	chr9:95798326-95798526	GM12878	blood:	n/a	n/a
32	CTCF	chr9:95798420-95798570	GM12871	blood:	n/a	n/a
33	CTCF	chr9:95798480-95798630	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr9:95798500-95798650	NB4	blood:	n/a	n/a
35	CTCF	chr9:95798244-95798789	K562	blood:	n/a	n/a
36	CTCF	chr9:95798558-95798565	GM12878	blood:	n/a	n/a
37	CTCF	chr9:95798480-95798630	K562	blood:	n/a	n/a
38	CTCF	chr9:95798400-95798550	K562	blood:	n/a	n/a
39	CTCF	chr9:95798380-95798530	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr9:95783040-95783190	HAc	cerebellar:	n/a	n/a
41	CTCF	chr9:95798454-95798603	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:95798357-95798625	K562	blood:	n/a	n/a
43	CTCF	chr9:95798260-95798530	GM12867	blood:	n/a	n/a
44	CTCF	chr9:95795158-95795222	K562	blood:	n/a	n/a
45	CTCF	chr9:95798500-95798650	HEK293	kidney:	n/a	n/a
46	CTCF	chr9:95793834-95793975	GM12878	blood:	n/a	chr9:95793873-95793886
47	CTCF	chr9:95798400-95798550	HMF	breast:	n/a	n/a
48	CTCF	chr9:95793406-95793462	GM13976	blood:	n/a	n/a
49	CTCF	chr9:95783147-95783170	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:95790580-95790730	NB4	blood:	n/a	n/a

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95789507..95791144-chr9:95796339..95798660,2	K562	blood:
2	chr9:95786580..95788650-chr9:95793860..95795482,2	MCF-7	breast:
3	chr9:95792812..95795096-chr9:95844025..95846622,2	K562	blood:
4	chr9:95781868..95785677-chr9:95818293..95823029,4	MCF-7	breast:
5	chr9:95797004..95799082-chr9:95868699..95871377,2	K562	blood:
6	chr9:95786084..95787782-chr9:95793550..95796411,2	K562	blood:
7	chr9:95762106..95765077-chr9:95786867..95789885,3	MCF-7	breast:
8	chr9:95781146..95783755-chr9:95792336..95795083,2	K562	blood:
9	chr9:95786580..95788650-chr9:95793860..95795482,2	MCF-7	breast:
10	chr9:95787005..95788972-chr9:95815833..95817820,2	MCF-7	breast:
11	chr9:95775081..95777481-chr9:95781149..95784106,3	MCF-7	breast:
12	chr9:95786084..95787782-chr9:95793550..95796411,2	K562	blood:
13	chr9:95789507..95791144-chr9:95796339..95798660,2	K562	blood:
14	chr9:95789704..95791224-chr9:95894882..95896881,2	MCF-7	breast:
15	chr9:95782537..95784143-chr9:95785904..95788136,2	K562	blood:
16	chr9:95775051..95776669-chr9:95785985..95787695,2	MCF-7	breast:
17	chr9:95773730..95778717-chr9:95778943..95783002,4	K562	blood:
18	chr9:95786380..95788403-chr9:95858223..95860085,2	MCF-7	breast:
19	chr9:95795050..95797966-chr9:95820852..95822454,2	MCF-7	breast:
20	chr9:95780776..95784501-chr9:95797559..95801380,3	MCF-7	breast:
21	chr9:95780776..95784501-chr9:95797559..95801380,3	MCF-7	breast:
22	chr9:95766059..95768538-chr9:95781716..95783313,2	MCF-7	breast:
23	chr9:95797648..95801708-chr9:95856413..95859083,5	MCF-7	breast:
24	chr9:95786796..95788401-chr9:95794963..95797802,2	MCF-7	breast:
25	chr9:95797817..95800116-chr9:95854194..95855844,2	MCF-7	breast:
26	chr9:95781146..95783755-chr9:95792336..95795083,2	K562	blood:
27	chr9:95768818..95771189-chr9:95783701..95785412,2	MCF-7	breast:
28	chr9:95791411..95794235-chr9:95796485..95798607,3	K562	blood:
29	chr9:95764926..95767414-chr9:95782606..95784200,2	MCF-7	breast:
30	chr9:95787650..95789848-chr9:96075432..96077120,2	MCF-7	breast:
31	chr9:95782411..95784335-chr9:95855706..95857608,2	K562	blood:
32	chr9:95782537..95784143-chr9:95785904..95788136,2	K562	blood:
33	chr9:95797721..95799808-chr9:95800868..95803137,2	MCF-7	breast:
34	chr9:95793756..95796104-chr9:95801423..95803382,2	MCF-7	breast:
35	chr9:95795131..95797013-chr9:95818973..95820858,2	K562	blood:
36	chr9:95526508..95528602-chr9:95789218..95791812,2	MCF-7	breast:
37	chr9:95786796..95788401-chr9:95794963..95797802,2	MCF-7	breast:

No data

Variant related genes	Relation type
FGD3	TF binding region
ENSG00000131669	chromatin interactions
ENSG00000165233	chromatin interactions
ENSG00000185963	chromatin interactions
ENSG00000127084	chromatin interactions
ENSG00000223446	chromatin interactions
ENSG00000157303	chromatin interactions

Extended variants
information (count: 723 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11790517	chr9:95782667-95782668	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192951780	chr9:95782680-95782681	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs202172343	chr9:95782681-95782682	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377126697	chr9:95782721-95782722	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371213207	chr9:95782722-95782723	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369033346	chr9:95782737-95782738	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372958884	chr9:95782738-95782739	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376439025	chr9:95782747-95782748	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115867184	chr9:95782748-95782749	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551049098	chr9:95782762-95782763	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376551260	chr9:95782779-95782780	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533868730	chr9:95782794-95782795	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs73514111	chr9:95782844-95782845	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369344672	chr9:95782920-95782921	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567843395	chr9:95782975-95782976	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs6479446	chr9:95782991-95782992	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs116740693	chr9:95782998-95782999	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs568291440	chr9:95783031-95783032	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs578160405	chr9:95783076-95783077	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs55903042	chr9:95783091-95783092	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs10992581	chr9:95783158-95783159	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572150697	chr9:95783161-95783162	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10992582	chr9:95783184-95783185	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs561075767	chr9:95783193-95783194	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150184064	chr9:95783195-95783196	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559724811	chr9:95783210-95783211	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78194631	chr9:95783223-95783224	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562712712	chr9:95783228-95783229	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533032081	chr9:95783234-95783235	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183847896	chr9:95783235-95783236	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs117639572	chr9:95783288-95783289	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527316893	chr9:95783331-95783332	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549076446	chr9:95783342-95783343	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567338924	chr9:95783355-95783356	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537960067	chr9:95783396-95783397	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs188181068	chr9:95783397-95783398	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs7872199	chr9:95783398-95783399	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs75165899	chr9:95783426-95783427	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs180691803	chr9:95783474-95783475	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373826677	chr9:95783475-95783476	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183619948	chr9:95783533-95783534	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs536218811	chr9:95783579-95783580	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554560244	chr9:95783588-95783589	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375643935	chr9:95783599-95783600	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370116347	chr9:95783673-95783674	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565991418	chr9:95783689-95783690	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190807351	chr9:95783741-95783742	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543900742	chr9:95783743-95783744	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562539368	chr9:95783744-95783745	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577808020	chr9:95783762-95783763	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95761600-95785800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr9:95761600-95785800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr9:95762000-95786400	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr9:95762600-95790200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:95763600-95787200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:95763800-95789400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:95766400-95785600	Strong transcription	Primary B cells from peripheral blood	blood
8	chr9:95766600-95783400	Weak transcription	Placenta	Placenta
9	chr9:95766600-95790400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:95766600-95790800	Weak transcription	Right Ventricle	heart
11	chr9:95766600-95791000	Weak transcription	Colonic Mucosa	Colon
12	chr9:95766600-95791000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr9:95766600-95794000	Weak transcription	Brain Hippocampus Middle	brain
14	chr9:95766800-95786400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr9:95767000-95787200	Strong transcription	Fetal Thymus	thymus
16	chr9:95770200-95793600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:95772600-95783000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr9:95773400-95786600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:95773600-95783000	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:95774200-95783800	Weak transcription	Fetal Brain Male	brain
21	chr9:95774800-95788400	Strong transcription	Thymus	Thymus
22	chr9:95775000-95786600	Strong transcription	Primary B cells from cord blood	blood
23	chr9:95776400-95783200	Weak transcription	Fetal Brain Female	brain
24	chr9:95776600-95799200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr9:95776600-95799400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:95776800-95783200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr9:95778000-95786600	Strong transcription	Spleen	Spleen
28	chr9:95778400-95783200	Weak transcription	Esophagus	oesophagus
29	chr9:95778600-95783000	Weak transcription	Fetal Stomach	stomach
30	chr9:95778600-95786400	Weak transcription	Gastric	stomach
31	chr9:95779000-95783600	Weak transcription	Small Intestine	intestine
32	chr9:95779600-95785800	Strong transcription	Fetal Intestine Large	intestine
33	chr9:95779600-95786600	Strong transcription	Dnd41	blood
34	chr9:95779600-95788800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
35	chr9:95779600-95798400	Strong transcription	Brain Germinal Matrix	brain
36	chr9:95780800-95787800	Strong transcription	Primary hematopoietic stem cells	blood
37	chr9:95781000-95786400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr9:95781000-95786600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr9:95781200-95789400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
40	chr9:95781400-95784000	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr9:95781600-95783200	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr9:95781600-95783400	Strong transcription	Adipose Nuclei	Adipose
43	chr9:95781600-95784200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr9:95781600-95785000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr9:95781600-95785600	Strong transcription	GM12878-XiMat	blood
46	chr9:95781600-95785800	Strong transcription	Duodenum Mucosa	Duodenum
47	chr9:95781600-95787200	Strong transcription	Fetal Intestine Small	intestine
48	chr9:95781600-95788800	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr9:95781800-95784000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr9:95781800-95786000	Strong transcription	Pancreas	Pancrea

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